Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_assertion evidence source_evidence_literature NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_assertion SIO_000772 23603762 NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_assertion wasDerivedFrom befree-20140225 NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_assertion wasGeneratedBy ECO_0000203 NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925930.RAw3RZ1PO2U1HLW9G3QjVOHfoPZ4PfD7kAPq_uL2Zxcl8130_provenance.